Time-resolved photoelectron imaging of S2 → S1 internal conversion in benzene and toluene

被引:54
|
作者
Suzuki, Yoshi-Ichi [1 ,2 ,3 ]
Horio, Takuya [1 ,2 ,3 ]
Fuji, Takao [1 ,3 ]
Suzuki, Toshinori [1 ,2 ,3 ]
机构
[1] Japan Sci & Technol Agcy, CREST, Chiyoda Ku, Tokyo 1020075, Japan
[2] Kyoto Univ, Grad Sch Sci, Dept Chem, Kyoto 6068502, Japan
[3] RIKEN Adv Sci Inst, Chem Dynam Lab, Wako, Saitama 3510198, Japan
来源
JOURNAL OF CHEMICAL PHYSICS | 2011年 / 134卷 / 18期
关键词
VIBRATIONAL-ENERGY REDISTRIBUTION; EXCITED-STATES; ANGULAR-DISTRIBUTIONS; VALENCE PHOTOIONIZATION; POLYATOMIC-MOLECULES; FLUORESCENCE-SPECTRA; DEWAR-BENZENE; SPECTROSCOPY; DYNAMICS; IONIZATION;
D O I
10.1063/1.3586809
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ultrafast internal conversion of benzene and toluene from the S-2 states was studied by time-resolved photoelectron imaging with a time resolution of 22 fs. Time-energy maps of the photoelectron intensity and the angular anisotropy were generated from a series of photoelectron images. The photoelectron kinetic energy distribution exhibits a rapid energy shift and intensity revival, which indicates nuclear motion on the S-2 adiabatic surface, while the ultrafast evolution of the angular anisotropy revealed a change in the electronic character of the S-2 adiabatic surface. From their decay profiles of the total photoelectron intensity, the time constants of 48 +/- 4 and 62 +/- 4 fs were determined for the population decay from the S-2 states in benzene and toluene, respectively. (c) 2011 American Institute of Physics. [doi: 10.1063/1.3586809]
引用
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页数:8
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